Variant #0000259447 (NC_000017.10:g.19552312C>G, NM_000382.2:c.28C>G (ALDH3A2))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.19552312C>G |
| DNA change (hg38) |
g.19648999C>G |
| Published as |
ALDH3A2(NM_000382.2):c.28C>G (p.(Gln10Glu)), ALDH3A2(NM_000382.3):c.28C>G (p.Q10E), ALDH3A2(NM_001031806.2):c.28C>G (p.Q10E) |
| ISCN |
- |
| DB-ID |
ALDH3A2_000089 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0036 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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